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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1182417 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type: C  {! N2 f, V% v' O
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
8 H  J  v' O$ c7 d, f+ Author Affiliations
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5 X9 u- X  R8 H) U4 M) z. v; |, i1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
4 }3 X) b* V5 n8 A. Z2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 5 m. x5 M7 e# t; O2 h
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
- y; j- x( O* d4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
  V2 W$ I& Q5 V/ ]7 o0 M5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
2 F( G* V' g8 y5 H7 S! ~6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
0 r. g- e! T/ i3 u  z7Kinki University School of Medicine, Osaka 589-8511, Japan
( K2 N9 q4 l' g* E+ `4 t: \8Izumi Municipal Hospital, Osaka 594-0071, Japan
4 j* J( h/ f4 B6 M9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 3 |9 H6 P$ J) R: _- m# m6 F; b, a
Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
4 r1 z, \& v$ c- h" e1 z; DAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. 4 ^, }1 H; Q' ~

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato . Z( C# }# E' ^" b% b1 S5 P
$ s0 w' S9 s( W& h; x8 \( U4 D- Z; f
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  , t" w* i8 D, d' j, Q$ ^
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Published online on: Thursday, December 1, 2011
1 s9 m$ _; f6 G9 o* ?% m0 O$ Q1 W! o6 z$ A* }; \9 t0 O0 ~& v
Doi: 10.3892/ol.2011.507
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Pages: 405-410 - n8 t. H5 U8 b6 b! V
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Abstract:' H  f9 a; {; m, B: V& n& i5 l
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.$ d9 e% t1 {$ I3 S
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population$ d4 r2 G" N- A8 O8 K6 u
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 5 L8 A5 I3 a) N" g3 w
+ Author Affiliations
5 I/ A4 m: n0 N% q" k, \* W1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 5 b, \2 m8 A% m& \0 @- x. S
2Department of Thoracic Surgery, Kyoto University, Kyoto
# [6 W! `% {& n  L' j3 Z3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
! c# C; t9 I3 `5 Z& ~9 G* W&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
3 F, b6 R7 Y0 c, W2 Q- f8 A% vReceived September 3, 2010. - F2 v6 l) s" L& H  j6 b
Revision received November 11, 2010. : V! `$ G6 {& d" E+ f0 j
Accepted November 17, 2010.
- |/ R+ Z7 S, v" a4 aAbstract
- u% @9 G9 B. l/ kBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. ) [( j2 e! Z" a" H# p! J
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. ' J: n9 L. V: Z% a) s  X
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
( S" E+ O* i: g. |- L; f" \* IConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 7 ~. \, G! \/ R$ i6 e& O6 d( H
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。- a. y  O1 c+ j- @2 U$ z7 ^
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?! p% y" V- g& W0 |& `8 ?
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
2 m9 C4 Z3 p2 w% L# w' h/ ^: f% mhttp://clinicaltrials.gov/ct2/show/NCT01523587/ E4 p% e% X+ o8 @+ P
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC1 w3 n. S/ I8 D8 l; W
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 ' l/ n7 t) U* k# H% t
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
8 u/ {" [$ t# u6 q- Z至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53 : T, ~1 y- m6 X3 ^* [0 G' x
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。( x9 K7 M  H9 `+ l# @( _
至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。" h, ~4 g# W  C6 @5 |/ |: z! ^5 F% }
不错。

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