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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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1249316 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- V* l' }/ x0 Y- }- v. ~: K* j
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
1 s4 Z1 h3 T( L* p+ Author Affiliations
1 [2 b' ?- B2 _) y; ]& T: E, J" t" K9 ~$ \2 t. `- l% [' I
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
1 S7 I# r% l2 Z* `9 |2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
( k- \/ D, R, m+ n  ?; v2 R" N0 k3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
% Z' v6 O, W9 y! D# p6 c) {& D; b6 ~) w4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
8 S8 N7 V% H2 B# w( r% y( P4 T5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 4 R8 q( B5 S& H0 r& d" `( }6 s
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
2 ?) E5 }( U  f- J" l7Kinki University School of Medicine, Osaka 589-8511, Japan
% m3 [0 G/ r& r. p( [8Izumi Municipal Hospital, Osaka 594-0071, Japan
$ D0 ^1 Q$ _3 \) d; e9 n9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
1 Z( {$ w2 |, P6 l3 f: }( mCorrespondence 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 / e, P/ u0 M% C( v8 p5 f9 i$ z
AbstractBackground: 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. / I' P% j8 N, f8 k9 R

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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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9 P+ O9 w5 w+ P+ a4 E: eAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato : L9 p3 U3 W1 O

% v* J9 N( b1 xAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  7 V2 J* V1 V& s- o) O6 Y
1 i/ l6 K/ X! ^* s" |
Published online on: Thursday, December 1, 2011 ' J/ }" |) l" B) C
) H1 [# `0 Q4 r8 I5 c
Doi: 10.3892/ol.2011.507
4 G0 X5 C6 ^  q3 o2 {' T6 {2 T- g' f0 A" I' _6 Q, A
Pages: 405-410 4 c6 x9 ]4 T6 w6 Y( W2 {
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Abstract:6 k9 m) U( [# d. C
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.
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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
' p8 ?( r- V, r; o$ `F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 0 f. w+ M4 G: m) ]7 d+ |/ \
+ Author Affiliations
$ ]3 ?: ]( ^0 H1 D' g2 X$ |1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
  D* B! L; e, R* s1 w' t2Department of Thoracic Surgery, Kyoto University, Kyoto 7 B* E4 l/ ?& b6 K
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
. _3 z. M, L6 m6 p0 V&#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 % P- ^( r# J! v$ A! l  `' P' Q
Received September 3, 2010.
6 C5 D4 a% ?% z; k( h. N' rRevision received November 11, 2010.
1 V9 q, f( L2 g: Q- p: F5 vAccepted November 17, 2010. # g" G3 A( e' S6 |# F* [" ^2 F/ n
Abstract
3 j! x7 h' z' y' `9 YBackground: 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. . x* k7 I4 c' u7 I; k0 o5 w
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. ! _7 x5 b0 Y7 {' U% j" k; T
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. 3 z& e& G( ?6 ?. t; n
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 6 Z  Y, V- W$ T9 q& ]
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。
& g  B# H% F3 v% G* }! B1 x. X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?4 k$ R4 s( _) f" S
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
$ F9 Y; T5 L" K0 _http://clinicaltrials.gov/ct2/show/NCT01523587
3 B8 Z5 L3 ?0 u. |+ e9 E; h2 g5 b$ X
- N$ L: x4 o! _5 }% e8 bBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC2 a6 |' K+ a8 }8 b8 D4 V: ^
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 5 V" u% S5 g! ^2 x

4 p* R6 g) K' y5 V. W7 s3 ]. _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。; P. T4 J( s% o! Z( K6 l
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
0 x( k# [- c9 H9 D5 ^/ m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。" D& Z5 p' l) g% A1 C- r/ ]
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。
- U! Q' Q" \' P% M9 q! U! O不错。

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