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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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1399860 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
! Z9 G, Z; _3 `/ K; I8 MNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
! g# x& Y2 j+ e+ Author Affiliations" Y; V; h/ F0 f2 u

0 Y5 ~6 ~% Y% R$ u6 d% D& o1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
1 d' W& G7 d7 C2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
5 \" A  r$ U! g0 Y0 U3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan * I: r7 L% A1 s+ W" \/ e# I( p
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 0 p' z" a' F; i/ H! o7 z
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 7 R0 t7 u5 a7 P- r( v. M4 Y8 p/ h
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan - V! c6 W$ p& q0 F" x+ S( H$ Y8 X% Y
7Kinki University School of Medicine, Osaka 589-8511, Japan 6 J; {' M4 x! E- W( U
8Izumi Municipal Hospital, Osaka 594-0071, Japan
2 v* M% o3 P. O6 l9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
2 @; Y! g" m- qCorrespondence 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
; Q( u( Z. l6 y* mAbstractBackground: 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.
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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 - I. f( u3 W6 p1 p, S' N

, J- A1 j0 U2 @+ WAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato * [9 i) X- s/ m# Q7 x* }
: H) z7 h* A! J$ T+ ]
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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( y* h4 P* V( B2 z/ p' m4 JPublished online on: Thursday, December 1, 2011 9 d! B2 q" W. h6 w9 n4 T
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Doi: 10.3892/ol.2011.507 0 P% @5 U5 O& B: A9 k
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Pages: 405-410 1 Y# \. Z! q2 ]. z$ ?# |
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Abstract:: W! J+ V9 a# R0 g, `( 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.5 v( j( A: |  v4 v, v" ^, O' v: Q

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 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
3 O. f! G/ y% U) g+ QF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 * f" K. J& {- @1 y, r7 w. M; G
+ Author Affiliations
4 n, O1 ^# E, Q0 b7 N- _- [1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu & t$ x2 ?4 I* r7 y. z
2Department of Thoracic Surgery, Kyoto University, Kyoto
" m, H- X: h, [+ t. k3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ; ~9 Y8 E! u( E2 f/ Z
&#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
2 j& e5 v) u7 F: L% g& ~; FReceived September 3, 2010. * Q: T$ e, p6 }" k
Revision received November 11, 2010. ' J* P' C, \. O! C) h
Accepted November 17, 2010.
. s# C; C2 T) w$ D1 G# |& r9 KAbstract  V5 {- y1 A, Q6 [+ q! x1 Y( p
Background: 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.
/ ~2 C: G7 h/ R* o* h$ G9 p% NPatients 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. & a% `. O! c4 e' \! K3 W) Y
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. $ |  P' F" ^1 K$ Y3 c  Q6 Z
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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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。
4 N! j: z2 W1 @' `6 i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?7 o! q& ^+ {/ w) m2 m9 I
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
6 g( \8 R# W; g9 f8 ^http://clinicaltrials.gov/ct2/show/NCT01523587
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7 e- W2 }' Z& j0 K" Z+ nBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
* e, T2 j: ?+ K9 w+ J" i4 {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 ) H# O  ~% b; i6 K, `0 v: G: j
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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。
6 s( _& }4 X5 U- 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 7 [! Y1 ~7 l' C
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。: H. c6 e) M( \" t7 U  l& X) G
至今为止,未出 ...

2 B! F9 Z2 S. h" r+ l没有副作用是第一追求,效果显著是第二追求。6 x' q2 H. n2 E5 m" d/ L% H1 D
不错。

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